9-chloro-7-(2-fluorophenyl)-N-methyl-5H-pyrimido[5,4-d][2]benzazepine-2-acetamide

Base Information

Chemical Name:9-chloro-7-(2-fluorophenyl)-N-methyl-5H-pyrimido[5,4-d][2]benzazepine-2-acetamide
CAS No.:86712-06-3
Molecular Formula:C₂₁H₁₆ClFN₄O
Molecular Weight:394.836
Hs Code.:

Synonyms:9-chloro-7-(2-fluorophenyl)-N-methyl-5H-pyrimido[5,4-d][2]benzazepine-2-acetamide

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Chemical Property of 9-chloro-7-(2-fluorophenyl)-N-methyl-5H-pyrimido[5,4-d][2]benzazepine-2-acetamide

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Technology Process of 9-chloro-7-(2-fluorophenyl)-N-methyl-5H-pyrimido[5,4-d][2]benzazepine-2-acetamide

There total 6 articles about 9-chloro-7-(2-fluorophenyl)-N-methyl-5H-pyrimido[5,4-d][2]benzazepine-2-acetamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.0%

: 86712-04-1
ethyl 9-chloro-7-(2-fluorophenyl)-5H-pyrimido[5,4-d][2]benzazepine-2-acetate

: 74-89-5
methylamine

: 86712-06-3
9-chloro-7-(2-fluorophenyl)-N-methyl-5H-pyrimido[5,4-d][2]benzazepine-2-acetamide

Guidance literature:: In ethanol; for 18h;
DOI:10.1021/jm00365a008

Reference yield:

: 58583-07-6
8-chloro-1-(2-fluorophenyl)-3,4-dihydro-5H-2-benzazepin-5-one

: 86712-06-3
9-chloro-7-(2-fluorophenyl)-N-methyl-5H-pyrimido[5,4-d][2]benzazepine-2-acetamide

Guidance literature:: Multi-step reaction with 6 steps

1: 85 percent / dimethylformamide / 2 h / 80 - 85 °C

2: 76 percent / sodium methoxide / methanol; CH₂Cl₂ / Ambient temperature

3: 83 percent / aq. H₂SO₄ / 12 h / Heating

4: 73 percent / POCl₃ / 4 h / 100 °C

5: 1.) potassium tert-butoxide / 2.) 15 min, 2.) a) 110 deg C, 2 h, b) 140 deg C, 4 h

6: 92 percent / ethanol / 18 h

With sulfuric acid; potassium tert-butylate; sodium methylate; trichlorophosphate; In methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00365a008

Reference yield:

: 58582-30-2
8-chloro-1-(2-fluorophenyl)-3,4-dihydro-4-[(dimethylamino)methylene]-5H-2-benzazepin-5-one

: 86712-06-3
9-chloro-7-(2-fluorophenyl)-N-methyl-5H-pyrimido[5,4-d][2]benzazepine-2-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: 76 percent / sodium methoxide / methanol; CH₂Cl₂ / Ambient temperature

2: 83 percent / aq. H₂SO₄ / 12 h / Heating

3: 73 percent / POCl₃ / 4 h / 100 °C

4: 1.) potassium tert-butoxide / 2.) 15 min, 2.) a) 110 deg C, 2 h, b) 140 deg C, 4 h

5: 92 percent / ethanol / 18 h

With sulfuric acid; potassium tert-butylate; sodium methylate; trichlorophosphate; In methanol; ethanol; dichloromethane;
DOI:10.1021/jm00365a008